Method and apparatus for repairing a hernia

ABSTRACT

A hernia repair device, comprising: an inflatable balloon having an inflation tube, the inflation tube having a proximal end attached to said balloon and a distal end adapted to be extracted from the body, separately from the balloon, via an opening which is smaller than a laparoscopic opening; and a mesh removably attached to said balloon, wherein the inflation tube passes through the mesh.

RELATED APPLICATION/S

This application is a continuation-in-part of U.S. application Ser. No.11/577,343 which is a national phase of PCT/IL2005/001070 filed on Oct.9, 2005. This application is also a continuation-in-part ofPCT/IL2007/001463 filed on Nov. 2, 2007 and PCT/IL2008/001381 filed onOct. 17, 2007.

This application claims priority from U.S. provisional application No.61/051,017 filed on May 7, 2008, U.S. provisional application No.61/051,018 filed on May 7, 2008 and U.S. provisional application No.61/058,218 filed on Jun. 3, 2008.

The contents of all of the above documents are incorporated by referenceas if fully set forth herein.

FIELD AND BACKGROUND OF THE INVENTION

The present invention, in some embodiments thereof, relates to herniarepair and, more particularly, but not exclusively, to a method andapparatus for inserting, positioning, orienting and deploying a herniarepair mesh in the abdominal cavity.

There are many techniques known in the art for repairing a hernia. Themost common techniques over the last several years are tension freerepair techniques, in open surgery or laparoscopic surgery, in which amesh or patch is used to bridge the abdominal defect.

US 2008/0065229 to Adams discloses a patch for repairing intra-abdominaldefect and a bio-absorbable balloon for deployment of the patch in theabdominal cavity. In most of the disclosed embodiments, the balloon isleft in the abdominal cavity. FIGS. 11 and 12 show an embodiment inwhich the balloon surrounds the mesh or patch and the balloon is removedfrom the abdominal cavity after deployment of the patch. In thisembodiment the inflation tube is positioned at the side of the balloonand does not contact the mesh at all.

U.S. Pat. No. 6,679,900 to Kieturakis discloses a balloon, comprisingtwo sheets, having a tubular member extending into the balloon and agraft which is releasably retained to the balloon.

EP 1336 391 to Cabaniols discloses a hernial plate comprising a pocketwhich is formed from two textile layers and balloon like expansion meansfor ensuring the deployment of the pocket. The expansion means arereceived in a removable manner in the pocket and pass by reversibledeformation from a deployed configuration to a compact ballconfiguration. One of the textile layers has an orifice allowing thewithdrawal of the expansion means out of the pocket after deployment ofthe pocket.

The prior art also shows several techniques for winding a surgicalmaterial and inserting into the body.

For example, US 2002/082588 to McMahon teaches a laparoscopic apparatusfor inserting and applying a sheet of surgical material comprising: ahandle with a sleeve extending thereof and a divided spindle comprisingtwo elongate members forming jaws which are moveable between an openposition in which a sheet of surgical material may be placed between orremoved from the jaws and a closed position wherein the sheet may beengaged between the jaws and furled on the spindle.

Another device known in the art is the Bard* Composix* LIP MESH(Technique Guide, www.davol.com, copyright 2006) where the mesh isprovided with an introducer tool which may also serve as winding deviceThe tool comprises two rods between which the mesh is placed. A T-cap isprovided on the rods to ensure that the mesh is caught between the rods.The surgeon then firmly grips the mesh and the handle and rolls the meshon the tool. The T-cap is removed and the tool with the mesh rolledthereon is inserted into the abdominal cavity through a trocar.

Additional background art includes US 2004/0073257 to Spitz, U.S. Pat.No. 5,258,100 to Gianturco, WO 95/30374 to Moll, U.S. Pat. No. 5,176,692to Wilk, U.S. Pat. No. 5,865,728 to Moll, U.S. Pat. No. 6,258,113 toAdams, U.S. Pat. No. 6,302,897 to Rousseau, U.S. Pat. No. 5,368,602 tode la Torre, U.S. Pat. No. 4,685,447 to Iversen, WO 01/97713 to Solecki,U.S. Pat. No. 6,152,895 to Wilk, WO 2004/037123 to Xavier and U.S. Pat.No. 5,141,515 to Eberbach.

SUMMARY OF THE INVENTION

According to an aspect of some embodiments of the invention there isprovided a hernia repair kit comprising an inflatable balloon having aninflation tube, and a mesh removably attached to said balloon. In anexemplary embodiment the inflation tube is adapted to be extracted fromthe body, separately from said balloon, via an opening which has adiameter smaller than a laparoscopic opening. The balloon is optionallyextracted via the laparoscopic opening.

According to an aspect of some embodiments of the present inventionthere is provided a hernia repair device, comprising:

an inflatable balloon having an inflation tube, the inflation tubehaving a proximal end attached to said balloon and a distal end adaptedto be extracted from the body, separately from the balloon, via anopening which is smaller than a laparoscopic opening, and

a mesh removably attached to said balloon,

wherein the inflation tube passes through the mesh.

According to some embodiments of the invention, the extent of a shapeformed by the outermost edges of the balloon is no larger than theextent of the mesh. Optionally, the area of the balloon in its deflatedconfiguration is less than 20% of the area of the mesh.

According to some embodiments of the invention, the distal end of theinflation tube comprises a grasping element. Optionally, said graspingelement comprises a loop. According to some embodiments of theinvention, the distal end of the inflation tube comprises a relativelystiff element to enable penetration of the inflation tube through themesh. Optionally, said stiff element is not sharp enough to harm themesh. Optionally, said stiff element is not sharp enough to harm tissue.

According to some embodiments of the invention, the mesh comprises anumber of closely spaced openings and said inflation tube has a diametersmaller than said openings. Optionally, said inflation tube is flexible.Optionally, said inflation tube is stretchable.

According to some embodiments of the invention, the balloon wheninflated has a smaller extent in one direction than in the twodirections perpendicular to the one direction wherein the tube isattached to the balloon at a central region of a surface perpendicularto the smaller extent. Optionally, said balloon is made of a nonbio-absorbable material.

According to some embodiments of the invention, the balloon has aplurality of connected portions separated by open areas, the open areascomprising more than 50% of the area of a shape formed by the outermostedges of the balloon. Optionally, the inside of the balloon comprisesinflation fluid only.

According to some embodiments of the invention, the balloon isasymmetric in shape such that when the balloon is folded in half the twofolded parts do not overlap.

According to some embodiments of the invention, the balloon furthercomprises at least one coil for removably attaching the mesh to theballoon. According to come embodiment, the coil comprises a proximal endattached to the balloon and a distal end comprising a relatively stiffelement to enable penetration of the coil through the mesh. Optionally,said stiff element is not sharp enough to harm the mesh. Optionally,said stiff element is not sharp enough to harm tissue.

According to an aspect of some embodiments of the invention, there isprovided a hernia repair device, comprising:

an inflatable balloon comprising a front side and a back side, whereinthe balloon comprises an inflation tube and at least one coil, the coilbeing attached at its back side; and

a mesh removably attached to said balloon by said at least one coil andsubstantially covering the front side of the balloon,

wherein the inflation tube passes through the mesh.

According to some embodiment of the invention, the mesh partially wrapsaround at least one edge of said balloon. Optionally, the major portionof the mesh is at the front side of the balloon.

According to an aspect of some embodiments of the invention, there isprovided a method of repairing a hernia, the method comprising:

inserting a balloon and a mesh into an abdominal cavity of a subject viaa laparoscopic opening, the balloon having an inflation tube whichpasses through the mesh;

catching and removing at least a portion of the inflation tube of theballoon from the abdomen via another opening in the hernia;

inflating the balloon;

positioning the mesh by pulling on the inflation tube, such that themesh is positioned at and close to the hernia; and

attaching the mesh to the abdominal inner wall over the hernia.

According to some embodiments of the invention, cutting the inflationtube from the balloon while the tube is situated outside the body viasaid other opening. According to some embodiments of the invention, themethod further comprises removing the balloon through the laparoscopicopening. Optionally, the balloon is removed after the mesh is attachedto the abdominal wall.

According to an aspects of some embodiments of the invention, there isfurther provided a method of repairing a hernia, the method comprising:

inserting a balloon and a mesh into an abdominal cavity of a subject viaa laparoscopic opening, the balloon having an inflation tube and themesh being removably attached to the balloon such that the inflationtube passes through the mesh;

inflating the balloon;

positioning the mesh in the abdominal cavity over the hernia by pulingthe inflation tube;

attaching the mesh to the abdominal wall; and

removing the balloon from the abdomen.

According to some embodiments of the invention, the balloon is removedfrom the abdomen after the mesh is attached to the abdominal wall.Optionally, the method further comprises folding and winding saidballoon and mesh before inserting to the abdominal cavity.

According to some embodiments of the invention, said balloon has aplurality of connected portions separated by open areas and whereinattaching the mesh to the abdominal wall comprises attaching throughsaid open areas.

According to an aspect of some embodiments of the invention, there isprovided a method of attaching a mesh to a hernia, comprising:

providing a balloon having at least one flexible coil attached theretoand a mesh attached to the balloon by passing said at least one coilthrough the mesh;

then positioning the mesh and balloon over the hernia such that the meshfaces the hernia;

then attaching the mesh to tissue surrounding the hernia;

then pulling said balloon away from the mesh thereby removing said atleast one coil from said mesh.

According to some embodiments, said mesh is formed of a plurality ofclosely spaced openings and said coil has a diameter smaller than saidopenings. Optionally, attaching the mesh to tissue comprises attachingwhile the balloon is inflated.

According to some embodiments of the invention, the coil is comprised ofa thin wire and wherein mesh is attached to the balloon by passing thewire through the mesh such that the mesh is held by the windings of thecoil.

According to an additional aspect of some embodiments of the invention,there is provided a winding device, for winding a mesh on rods,comprising:

two elongated rods;

a handle attached to the distal ends of said rods, the handle beingconvertible into an anchor adapted to anchor the rods when winding themesh on the rods; and

a knob attached to the proximal ends of the rods adapted to rotate therods.

According to some embodiments, the winding device further comprises ajoint between the handle and the rods, the joint being bendable adaptedto change the angle between the rods and the handle. Optionally, thehandle can be removed from the distal end of the rods and the handle isadapted to be attached to the knob.

According to an aspect of some embodiments of the invention, there isprovided a winding device, comprising:

two elongated rods;

a handle attached to the distal ends of said rods; and

a knob attached to the proximal ends of the rods,

wherein the winding device further comprises a bearing between thehandle and rods such that the rods can be rolled without moving thehandle.

Unless otherwise defined, all technical and/or scientific terms usedherein have the same meaning as commonly understood by one of ordinaryskill in the art to which the invention pertains. Although methods andmaterials similar or equivalent to those described herein can be used inthe practice or testing of embodiments of the invention, exemplarymethods and/or materials are described below. In case of conflict, thepatent specification, including definitions, will control. In addition,the materials, methods, and examples are illustrative only and are notintended to be necessarily limiting.

BRIEF DESCRIPTION OF THE DRAWINGS

Some embodiments of the invention are herein described, by way ofexample only, with reference to the accompanying drawings. With specificreference now to the drawings in detail, it is stressed that theparticulars shown are by way of example and for purposes of illustrativediscussion of embodiments of the invention. In this regard, thedescription taken with the drawings makes apparent to those skilled inthe art how embodiments of the invention may be practiced.

In the drawings:

FIGS. 1A-1D are schematic illustrations of a balloon with inflation tubein accordance with exemplary embodiments of the invention;

FIGS. 2A-2H are schematic illustrations of a balloon with coils forattaching the balloon to the mesh in accordance with exemplaryembodiments of the invention;

FIGS. 3A-3B are schematic illustrations of a balloon attached to a meshin accordance with another exemplary embodiment of the invention;

FIGS. 4A-4B are schematic illustrations of a folded balloon and mesh inaccordance with an exemplary embodiment of the invention;

FIG. 5 is a schematic illustration of a winding device in accordancewith an exemplary embodiment of the invention;

FIG. 6 is a flowchart of a method of winding surgical material on thewinding device of FIG. 5;

FIGS. 7A-7I are schematic illustrations of acts of the method of FIG. 6;

FIGS. 8A-8D are schematic illustrations of a winding device having ahandle which is used as an anchor in accordance with an exemplaryembodiment of the invention;

FIGS. 9A-9M are schematic illustrations of a winding device inaccordance with another exemplary embodiment of the invention;

FIG. 10 is a flowchart of a method of treating a hernia in accordancewith an exemplary embodiment of the invention; and

FIGS. 11A-I are schematic illustrations of acts of the method of FIG.10.

DESCRIPTION OF EMBODIMENTS OF THE INVENTION

The present invention, in some embodiments thereof, relates to herniarepair and, more particularly, but not exclusively, to a method andapparatus for inserting, positioning and deploying a hernia repair meshin the abdominal cavity.

A mesh, as referred to herein, relates to a mesh or patch used to repaira hole or hernial defect. Optionally, the mesh is formed by materialsurrounding closely spaced holes or openings. Alternatively, the mesh orpatch is made of a homogenous fabric. In such a mesh, the holes oropenings in the fabric may be invisible to the human eye. The fabric ormaterial may be a polymeric composition or one or more of glass fibre;metal fibre such as titanium, stainless steel, nitinol (Nickel Titaniumalloys); cardboard; natural fiber; polyester; polypropylene; silicone;rubber or rubber-like compositions. Optionally, the mesh has a coatingon one side, for example a coating for preventing bowel adhesion whenthe (other side of the) mesh is attached to the abdominal wall. In anexemplary embodiment, the mesh and/or coating are bioabsorbable.

An aspect of some embodiments of the invention relates to a balloonremovably attached to a mesh. A balloon, as used herein refers to aninflatable container of any size, shape or material. For example, theballoon can be made of one or more of rubber, latex, silicone,polyurethane, chloroprene, a nylon fabric and a thermoelastomericmaterial. The balloon can be made of biocompatible materials, non-bioabsorbable materials, self-dissolving materials or shape memorymaterials.

In an exemplary embodiment, the balloon comprises an inflation tubewhich passes through the mesh. Optionally, the inflation tube is aflexible inflation tube. Alternatively or additionally, the inflationtube is stretchable.

An aspect of some embodiments of the invention relates to methods ofhernia repair. In an exemplary embodiment, a balloon and mesh areinserted into the abdominal cavity via a trocar or via a laparoscopicopening. As used herein, the term laparoscopic opening refers to atrocar incision into the body. Optionally, a laparoscopic opening has adiameter of between 3-20 mm, between 3-18 mm or between 5-18 mm, forexample about 3, 5, 10, 15, 18, 20 mm or more.

The balloon comprises an inflation tube which is preferably insertedwith the rest of the balloon into the abdominal cavity. Optionally, theentire inflation tube is inserted into the abdominal cavity. In anexemplary embodiment, the inflation tube of the balloon is caught andthe end not attached to the balloon is removed from the abdominal cavitythrough another opening, different than the laparoscopic opening.Optionally, the inflation tube is caught with a suture passer throughthe different opening. Optionally, the inflation tube is caught with adifferent grasping device through the different opening. Optionally, thedifferent opening is smaller than a laparoscopic opening. The differentopening may be made through the hernial defect or in the tissueimmediately surrounding the hernia defect. Optionally, the differentopening is substantially smaller than the laparoscopic opening. Forexample, the different opening can have a diameter of or less than about1, 2, 2.5 or 2.9 mm. Due to the small size of the opening, the differentopening is not harmful to the hernial defect and/or the tissuesurrounding the defect.

In an exemplary embodiment the balloon is inflated, thereby deployingthe mesh. Preferably, the balloon and mesh are positioned in theabdominal cavity by pulling on the inflation tube, optionally throughthe different opening, for example, a small opening in the hernia. In anexemplary embodiment the mesh is attached to the abdominal wall and theballoon is deflated and removed from the abdominal cavity. Optionally,the mesh is attached to the abdominal wall before deflation of theballoon. Optionally, the balloon is removed via the laparoscopicopening. Optionally, the mesh is attached to the abdominal wall usingstaples, tacks, sutures or other methods known in the art. In anexemplary embodiment the staples or tacks are provided to the mesh viaopen areas in the balloon and/or via surroundings of the balloon.

It is understood that if the tube is attached near the center of theballoon, then by pulling on the tube via the smaller hole in the hernia,the balloon (and the mesh) are automatically positioned on the hernia.

In an exemplary embodiment of the invention the balloon comprises atleast one flexible coil attached thereto for removably attaching themesh to the balloon. The term coil as used herein refers to a flexibleand/or elastic object which is preferably retractable. Optionally, thecoil is made of one or more of plastic, nylon, polyurethane and metalwire and has a spiral shape when retracted and a generally linear shapewhen stretched.

Optionally, the mesh comprises a plurality of closely spaced holes (orspaces between fibers for a woven mesh) and the wire has a diametersmaller than the holes or spaces. When stretching the coil, the spiralcontour of the coil narrows, thereby decreasing its diameter.Optionally, the decreased spiral diameter is adapted to pass through theholes in the mesh. Alternatively or additionally, the narrow spiralassists in threading the wire through the holes of the mesh. Preferably,the wire diameter is smaller than the dimensions of the holes in themesh.

Optionally, the balloon is removed from the mesh and abdominal cavity bypulling the balloon away from the mesh thereby removing said at leastone coil from said mesh. Optionally, the balloon is attached to andremoved from said mesh by attachment means as disclosed inPCT/IL2008/001381 filed on Oct. 22, 2008, published as WO 2009/050717,the disclosure of which is incorporated herein by reference.

In an exemplary embodiment, the inflation tube and/or coil comprise astiff end, such as a needle, at its end for ease of penetration throughthe mesh. The stiff end is optionally made of one or more of plastic,metal, nylon and polyurethane. Optionally, the stiff end is cut offafter penetration through the mesh. Optionally, the stiff end is notsharp enough to harm tissue or the mesh or the balloon, such that whenthe stiff end is not cut off after penetration through the mesh, thestiff end will not harm a tissue.

Alternatively or additionally, the inflation tube has a diameter adaptedto pass through any of the holes of the mesh. Optionally, the mesh has aspecial opening at a central region thereof, adapted for insertion ofthe inflation tube.

In an exemplary embodiment the inflation tube further comprises agrasping appendage to enable grasping of the inflation tube in theabdominal cavity. Optionally, the grasping appendage comprises a loop.Alternatively or additionally, the grasping appendage comprises saidneedle. In an embodiment of the invention, a small opening is made inthe hernia and the inflation tube is caught via the small opening andbrought outside the body. After the mesh is positioned and preferablyafter it is attached to the abdominal wall, the inflation tube isoptionally cut off near the abdomen.

Optionally, the mesh is situated only on one side of the balloon whenthe balloon is inflated. Alternatively, the mesh wraps around theborders of the balloon and is attached at the backside of the balloon,i.e. the side opposite to the side where the inflation tube is attachedto, preferably only near the outer edges of the balloon. This enablesthe balloon to provide full support to the mesh when inflated and todeploy the edges of the mesh as well as the center thereof. Optionally,in this embodiment, the mesh partially wraps the balloon and the majorportion of the mesh is at the front side of the balloon, i.e. the sidefacing the hernia.

In an exemplary embodiment of the invention, the inside of the balloonincludes inflation fluid only. Inflation fluid, as used herein, includesliquid, gel and/or gas. Optionally, the inflation tube does notpenetrate into the balloon.

In an exemplary embodiment, the area of the balloon in its deflatedstate is no larger than the area of the mesh. Optionally, the area ofthe balloon comprises no more than 70%, 50%, 20%, 10%, 5% or anyintervening number, of the area of the mesh. Optionally, the balloon hasa plurality of connected portions separated by open areas, the openareas comprising at least 70%, 50% or 30% of the extent of the balloon.The extent of the balloon, as used herein refers to the extent of ashape formed by the outermost edges of the balloon. The open area(s)refers to that portion of the extent that is not covered by the balloonmaterial, when inflated. Optionally, the extent of the balloon is nolarger than the extent of the mesh.

In an exemplary embodiment the balloon is wound into a roughlycylindrical shape before insertion in the abdominal cavity. Optionally,the balloon, with the mesh optionally attached thereto, is folded beforewinding in order to protect an optional coating of the mesh. Preferably,a non-adhesive coated portion of the mesh is folded on itself. It isnoted that folding the coated mesh of the balloon enables the right sideof the mesh to face the abdominal wall when deployed in the abdominalcavity. Optionally, the balloon has an asymmetric shape such that whenfolded the two folded parts of the balloon do not overlap, therebyproviding a relatively thin construction of the folded balloon. Thisenables the folded balloon structure to be smaller.

Alternatively or additionally, the balloon can have any one of abranching shape, an eccentric shape, a concentric shape, a closed shape,an open shape, a symmetric shape, or any combination thereof.

An aspect of some embodiments of the invention relates to a windingdevice for winding surgical material before insertion into the body.Optionally, the surgical material comprises a mesh and a balloonattached thereto.

In an exemplary embodiment, the winding device is adapted for insertionthrough a trocar for insertion of the wound surgical material into thebody. In an exemplary embodiment the winding device comprises two joinedrods which can be separated for placing the surgical material betweenthem. In an exemplary embodiment the winding device further comprises ahandle on the distal end of the rods. Preferably, the winding devicefurther comprises a knob on the proximal end-of the rods. Preferably,the knob comprises two attached parts which can be dismantled in orderto separate the rods and insert the surgical material between them.

Optionally, the handle can be deformed into an anchor which serves as abase for winding surgical material on the rods. Preferably, the anchorenables a surgeon or other single person to wind the surgical materialon the rods, without requiring assistance. Optionally, the handlecomprises two parallel parts, connected at their central portion and canbe moved to form an anchor. Optionally, the anchor has an X-shape, arectangular shape, a triangular shape or any other shape. Optionally,the parallel parts of the anchor comprise slits for anchoring the anchorto a tray or other base. In an exemplary embodiment, the handle can beremoved from the distal end and attached to the knob at the proximal endof the rods. This enables easy gripping of the winding device forinsertion into the body as well as clearing the path for the surgicalmaterial to be released in the body.

In an exemplary embodiment, the winding device further comprises abearing between the handle and rods such that the rods can be rolledwithout moving the handle or anchor. Optionally, the joint between thehandle and rods is bendable to ease winding the surgical material on therods, when the handle serves as an anchor.

For purposes of better understanding some embodiments of the presentinvention are illustrated in FIGS. 1-11 of the drawings.

Before explaining at least one embodiment of the invention in detail, itis to be understood that the invention is not necessarily limited in itsapplication to the details of construction and the arrangement of thecomponents and/or methods set forth in the following description and/orillustrated in the drawings and/or the Examples. The invention iscapable of other embodiments or of being practiced or carried out invarious ways.

FIG. 1A illustrates a balloon 100 in accordance with an exemplaryembodiment of the invention. Balloon 100 comprises an inflatable body110 and an inflation tube 120. In an exemplary embodiment of theinvention, body 110 has an asymmetric shape such that when the balloonis folded, as shown in FIG. 1B, the two folded parts of the balloon donot overlap. The non-overlapping parts provide a relative thinconstruction of the folded balloon. This is advantageous when theballoon is wound for insertion through a trocar into the abdominalcavity. It is well known that it is easier to insert small devicesthrough laparoscopic openings or trocars. The relatively thinconstruction of the folded balloon enables a thin construction of thewound roll and assists in the procedure.

Inflatable body 110 is shown having a plurality of connected portionsseparated by open areas 150. Optionally, the open areas comprise morethan 70%, 50% or 20% of the extent of the balloon. The extent of theballoon being defined as the extent of a shape formed by the outermostedges of the balloon, for example edges 109 in FIG. 1A. Alternatively oradditionally, the open areas comprise more than 30%, 50%, 70% or anyintervening number of the area of the balloon in its deflated and/orinflated state. The open areas of the balloon also assists in providinga thin construction of the wound balloon for insertion into theabdominal cavity as referred to above.

In an exemplary embodiment, inflation tube 120 is flexible.Alternatively or additionally, the inflation tube is stretchable.Preferably inflation tube 120 is attached at a central region ofinflatable body 110. Optionally, inflation tube 120 is attached to anouter surface of body 110 and does not penetrate into the balloon, suchthat the inside of body 110 comprises inflation fluid only.

FIG. 1C is a closer view of inflation tube 120 in accordance with anexemplary embodiment of the invention. Inflation tube 120 includes atube 122 and an optional grasping appendage 124. Grasping appendage 124is adapted to assist a surgeon in grasping the inflation tube in theabdominal cavity, optionally via a suture passer or other grasperinserted via a small hole in the hernia or in the tissue surrounding thehernia. Optionally, as shown in FIG. 1C, grasping appendage 124 is aloop. Alternatively, grasping appendage 124 can be any other suitablegrasping means known in the art. For example, a hook at the end of a rodcan be used to grasp appendage 124.

Optionally, inflation tube 120 further comprises a relatively stiff end126 for providing smooth penetration of inflation tube 120 through themesh. Stiff end 126 may comprise a needle or any other suitable sharpelement. Preferably, end 126 is not sharp enough to harm the mesh or theballoon. In addition, end 126 is optionally not sharp enough to harm atissue, such as the tissue in the abdominal cavity of the patient.Optionally, end 126 has a smaller diameter than tube 122.

FIG. 1D illustrates a balloon 111 according to another exemplaryembodiment of the invention. In this embodiment as well, the ballooncomprises an asymmetric shape. In addition, the balloon comprisesoutermost edges 107 which provide support for a mesh attached thereto,while providing large open areas 108, thereby providing a relative thinconstruction of the balloon when rolled. Balloon 111 may include aninflation tube similar to that of balloon 100.

In an exemplary embodiment of the invention, balloon 100 or 111 isremovably attached to a mesh with flexible coils, as shown in FIGS.2A-2H. FIG. 2A shows a balloon 100 having a plurality of coils 112 atits ends. In an exemplary embodiment, the balloon comprises at least onecoil. Optionally, the balloon comprises four coils at its ends.Alternatively, the balloon comprises an additional set of coils 114,which are positioned at a distance from its ends, as shown in FIG. 2A.This enables meshes of different sizes to be attached to the balloon,using different sets of coils.

FIG. 2B is a closer view of coils 112 and 114. Coils 112 and 114 arepositioned at an extension 136 of balloon 100. Coils 112 and 114 consistof a flexible coiling part 130 and an optional linear part 132.Optionally, coils 112 and 114 also comprise a relatively stiff element134, such as a needle or a sharpened end of the optional linear part orthe coiling part, for ease of penetration through a mesh.

As shown in FIG. 2C, coils 112 are adapted to be penetrated through amesh 200. Mesh 200 comprises closely spaced holes 202. For example, theholes are the spaces between adjacent warp and weft threads of the meshor the holes are formed within the fabric of which the mesh is made of.Optionally, the wire used to produce the coils 112, has a diameteradapted to pass through holes 202, optionally, the diameter is smallerthan holes 202. Optionally, inflation tube 120 also has a diametersmaller than holes 202 and passes through the holes.

Optionally, when the mesh has a coated side, care should be taken thatthe coated side should face the balloon. This is since the coated sideof the mesh should not face the hernia.

Coiling parts 130 are retractable and/or flexible and can optionally bestretched for penetrating through a mesh 200 as shown in FIG. 2D. Whenstretched, coiling parts 130 reduce in diameter, thereby assisting inpenetration-through the mesh. Preferably, coiling parts 130 areretractable and return to their original coiled shape after passingthrough mesh 200, as shown in FIG. 2E. The flexible characteristic ofcoiling part 130 also allows easy removal of the balloon from the mesh.By pulling the balloon, coiling parts 130 stretch and pass through holes202 of mesh 200, thereby removing balloon 100 from mesh 200, withoutharming mesh 200.

In an exemplary embodiment of the invention, linear part 132 and/orstiff element 134 are cut off after penetration through the mesh, asshown in FIG. 2F. Optionally, stiff element 126 of inflation tube 120 isalso cut off after being thread through the mesh.

FIGS. 2G and 2H illustrates a different coil 115 which can be used toattach the mesh to the balloon in accordance with another exemplaryembodiment of the invention. Coil 115 optionally also comprises arelatively stiff element 117 for threading through the mesh, similar tostiff element 134 of coil 112 discussed above. Optionally, coil 115further comprises a vertical element 118 which is attached to theballoon, as shown in FIG. 2D. Vertical element 118 preferably avoids thecoil from sliding out of the balloon. It is noted that while FIG. 2Hdepicts balloon 111, both coils 112 and 115 may be used with balloons110 and 111 or any other balloon known in the art.

Coil 115 has a flat configuration which may be advantage for providing athin construction of the rolled balloon.

Another exemplary embodiment of a construction for removably attachingballoon 100 to mesh 200 is shown in FIGS. 3A and 3B. In this embodiment,mesh 200 wraps around the edge of the balloon and is attached to a coil,for example coil 112 or 115. The coil extends from the back of theballoon, i.e. the side opposite that from which the tube extends, asshown in FIG. 3B. This embodiment enables greater support to the mesh,as opposed to the embodiment shown in FIG. 2. Optionally, in theembodiment of FIG. 3, the major part of the mesh is at the front side ofthe balloon, which faces the abdominal wall, such that the meshpartially wraps the balloon.

It is noted that FIGS. 2 and 3 are only exemplary means of removablyattaching the balloon to the mesh. Any other fixating means known in theart may be used, such as sutures, Velcro, glue and/or any other fixationmeans disclosed in PCT/IL2008/001381 filed on Oct. 22, 2008, publishedas WO 2009/050717, the disclosure of which is incorporated herein byreference.

FIGS. 4A-4B are schematic illustrations of a folded balloon and mesh inaccordance with an exemplary embodiment of the invention. Mesh 200 andballoon 100 are optionally folded such that inflation tube 120 isoutside the folded structure. Flexible inflation tube 120 can then bepositioned parallel to the fold, in order to be wound with the balloonand mesh, as described with reference to FIGS. 5-7 below. Optionally,the mesh has a non-adhesive coating and the mesh is folded such that thecoated side of one half faces the coated side of the other.

FIG. 5 is a schematic illustration of a winding device 500 in accordancewith an exemplary embodiment of the invention. Winding device comprisestwo closely positioned rods 520 and 530. At a distal end 522 of rods 520and 530, a handle 510 can be attached. Optionally, handle 510 isT-shaped. In an exemplary embodiment, the top of handle 510 comprisestwo parts, 512 and 514 which can be deployed into an anchor as describedin FIG. 8. The anchor can have an X-shape, a rectangular shape, atriangular shape or any combination of shapes thereof.

Handle 510 optionally further comprises a bearing 518 enabling rods 520and 530 to be rolled without rotating handle 510. A flexible joint 516is preferably provided between handle parts 512, 514 and bearing 518,allowing handle parts 512, 514 to be moved with respect to bearing 518thereby changing the angle between rods 520, 530 and handle 510.

At a proximal end 524 of rods 520, 530 there is preferably provided aknob 540 for ease of grasping of the rods proximal end.

FIG. 6 is a flowchart of a method of winding surgical material on thewinding device of FIG. 5. FIGS. 7A-7I are schematic illustrations of theacts listed in the flowchart of FIG. 6.

At 602 a winding device 500 and surgical material 200 are provided asshown in FIG. 7A. Surgical material 200 will be referred to hereinafteras mesh 200, however, it is understood that any other surgical materialcan be used. For example a folded balloon attached to a mesh as shown inFIG. 4B.

Rods 520 and 530, which are held tightly together, optionally by knob540, are released at 604 in order to insert mesh 200 between them.Optionally, knob 540 consists of two parts 542 and 544 which can bereleased, thereby providing an opening between rods 520 and 530, asshown in FIG. 7B.

An edge of mesh 200 is inserted through rods 520 and 530 at 606, asshown in FIG. 7C. Optionally, only a corner of the mesh is insertedthrough the rods. Rods 520 and 530 are pressed together to keep mesh 200firmly captured between the rods, at 608. FIG. 7D depicts two ends 542and 544 of knob 540 returned to its original position, thereby closingthe opening between rods 520 and 530.

Handle 510 is optionally attached to distal end 522 of rods 520, 530 at610. This provides easy grasping of the handle when rolling rods 520 and530 at 612.

In general, three hands are required to wind mesh 200 on rods 520, 530.A first hand is used to roll rods 520, by rolling knob 540. A secondhand is used to hold mesh to avoid wrinkles in the wound constructionand a third hand should be used to grasp handle 510 to stabilize windingdevice 500 during the winding process. In conventional winding devices,handle 510 rolls with the rods and therefore makes it difficult for anassistant to hold the handle during the winding process.

In an exemplary embodiment, when bearing 518 is provided between rods520, 530 and handle 510, the rods can be rolled without moving handle510. In this embodiment an assistant can help the surgeon in windingmesh 200. One person rolls the rods by rolling knob with one hand, whilehis second hand holds mesh to avoid wrinkles in the wound construction.The other person can hold handle 510 to stabilize the winding device.Alternatively, handle 510 can also serve as an anchor such that no thirdhand is required, as described below with respect to FIGS. 8A-8D.

FIG. 7F depicts winding device 500 while mesh 200 is wound onto rods 520and 530. After winding mesh 200, handle 510 is removed from the rods inorder to clear the path for mesh 200 to be released into the abdominalcavity, at 614. This is shown in FIG. 7G.

In an exemplary embodiment, at 616, handle 510 is then attached to knob540 as shown in FIG. 7H. Attaching handle 510 to knob 540 providesbetter grasping means and aids in maneuvering winding device 500 througha trocar into a laparoscopic opening and then releasing the mesh intothe abdominal cavity. Optionally, knob 540 has a protrusion 546 at itsend which fits into an aperture 548 of the handle, thereby attachinghandle 510 to knob 540, as shown in FIG. 7L Alternatively, any otherattaching means known in the art may be used, such as screws, velcro orglue.

At 618, winding device 500, with mesh 200 wound onto it, is insertedthrough a trocar into the abdominal cavity, as shown in FIG. 11A.

FIGS. 8A-8D are schematic illustrations of a winding device 800 having ahandle 510 which is used as an anchor in accordance with an exemplaryembodiment of the invention. FIG. 8A is a different view of theoptionally T-shaped handle 510 from that shown in FIG. 7E. Handle 510comprises two parts 512 and 514 attached with a hinge at their center513. In FIG. 8A, parts 512 and 514 are placed parallel to each other andform a single arm. Parts 512 and 514 can be rotated away from each otherand can be oriented substantially perpendicular to each other to form anX shape as shown in FIG. 8B. It is noted that any other shape suitablefor serving as an anchor may be used, such as a rectangular ortriangular shape.

Optionally, parts 512, 514 also comprise slits 515. Slits 515 areoptionally used for anchoring the handle to a tray 810 or other base asshown in FIG. 8D. The edge of the tray 810 are passed into slits 515,thereby anchoring handle 510 to tray 810.

In an exemplary embodiment, there is further provided a flexible joint516 between parts 512, 514 and bearing 518. Flexible joint 516 enableshandle 510 to be rotated with respect to bearing 518 thereby changingthe angle between rods 520, 530 and handle 510, as shown for example inFIG. 8C. This is another feature that enables handle 510 to be anchoredand stabilize winding device 500 during the winding process. With thisembodiment, a surgeon does not require any assistance in windingsurgical material onto rods 520, 530.

It is noted that winding devices 500 and 800 are only exemplary and themesh 200 and balloon 100 can be wound without a winding device or byused of any other winding device known in the art. For example, FIGS.9A-9N illustrate another winding device in accordance with anotherexemplary embodiment of the invention.

FIG. 9A is a schematic illustration of a winding device 900 inaccordance with an exemplary embodiment of the invention. Winding device900 is adapted to receive and wind surgical material 100, and/or 200.Winding device 900 consists of two bases 902, connected by two rods 901.A closer view of bases 902 is shown in FIG. 9B.

Base 902 has a bottom layer 903 and a top 905. Optionally, base 902includes a tray 910 extending from top 905, on which the surgicalmaterial can be placed. Base 902 preferably also includes an upper hole906 and a lower hole 908 for placement of a spool 904, as shown in FIG.9A. In an exemplary embodiment, device 900 consists of two spools 904between which the surgical material is placed and then wound on.Resilient stoppers 912 are optionally provided between holes 906 and908. Resilient stoppers 912 keep spool 904 in upper hole 906 as shown inFIG. 9A and are adapted to open when pushed from the top, such thatspool 904 can pass from upper hole 906 to lower hole 908 by pushing itdown.

FIG. 9C is a closer view of spool 904, depicting a rod 914 and a knob916. Knob 916 is preferably notched, such that a rod 926 of a secondspool 920 (shown in FIG. 9G) can be inserted in the notch. Optionally,knob 916 has a round shape as shown in FIG. 9C. Alternatively, knob 916has a hexagonal or other shape.

FIG. 9D shows winding device 900 with spool 904 placed in upper hole 906and a slotted tube 930 placed below lower hole 908, adapted to acceptspool 904 after the surgical material is wound to it, when pushed tolower hole 908. Optionally, tube 930 is elastic and spring-like. Ends932 of tube 930 are positioned in grooves 934 in order to keep tube 930in an open position. When tube 930 is pushed down, ends 932 are releasedfrom grooves 934 and tube 930 closes, as shown in FIG. 9L and describedbelow.

Winding device 900 is adapted to wind surgical material, such as mesh200 and/or balloon 100, as will be described below. The surgicalmaterial is inserted into a package 950 depicted in FIG. 9A. Package 950is adapted to keep surgical material 100,200 in place during the windingprocedure and is preferably made of thin polypropylene. Optionally,package 950 is made of any other suitable material or combination ofmaterials, such as nylon or metal, adapted to hold the surgicalmaterial. Package 950 preferably contains apertures 952 in its shapeadapted to be inserted through top 905 of base 902 and extensions 954adapted to be positioned on tray 910. Optionally, package 950 is placedon top of surgical material 100, 200, and is not enclosing the surgicalmaterial. Alternatively, package extension 954 comprise slits 955through which the surgical material is threaded, thereby secured inplace.

Reference is now made to FIGS. 9E-9N where the procedure of windingsurgical material with device 900 is shown.

FIG. 9E illustrates winding device 900 at a starting position, withsurgical material 100, 200 positioned on tray 910 (not visible sincecovered by the package). Second spool 920 is then added to device 900,as shown in FIG. 9F, such that the surgical material is positionedbetween spools 920 and 904, as shown in FIG. 9G. Spool 920 preferablyhas two knobs at its ends, adapted to be inserted into openings 924 indevice 900. Optionally, the device is configured such that when spools920 and 904 are positioned as shown in FIG. 9G, there is no spacebetween the rods of the spools.

Surgical material 100, 200 is then wound onto spools 904 and 920, byturning knobs 922, as shown in FIG. 9H. FIG. 9I depicts surgicalmaterial wound onto spools 904 and 920 while positioned in upper hole906.

Spools 904 and 920 are then pushed to lower hole 908, into tray 930, asshown in FIG. 9J. The spools are then pushed further down, whereby tray930 is also pushed down, upon which edges 932 of tray 930 are releasedfrom grooves 934 and tube 930 is closed, having surgical material 100,200 wound onto spools 904, 920 therein, as shown in FIG. 9K. At thispoint, knobs 916 and 922 are removed from one end of spools 904 and 920.This allows tube 930 to be removed from winding device 900 as shown inFIG. 9L. FIG. 9M is a closer view of tube 930 with surgical material100, 200 wound therein. In an exemplary embodiment, tube 930 is adaptedto be inserted into the body, optionally through a trocar.Alternatively, wound surgical material 100, 200 is removed from tube 930and/or spools 904, 920 before insertion into the abdominal cavity.Optionally, the surgeon may release the wound surgical material 100, 200after the stage described in FIG. 9I and insert it to the body,optionally through a trocar. Alternatively or additionally, one of theknobs 922 also comprises a longer handle, to ease the winding and theinsertion of surgical material 100, 200.

FIG. 10 is a flowchart of a method of treating a hernia in accordancewith an exemplary embodiment of the invention. FIGS. 11A-I are schematicillustrations of acts of the method outlined in FIG. 10.

At 1020, the mesh and balloon are inserted into the abdominal cavitythrough a laparoscopic opening and/or trocar. Optionally, as shown inFIG. 11A, mesh/patch 200 and balloon/inflatable container 100 areinserted while wound on winding device 500 or 800 or some other windingdevice, which is inserted through a trocar 1100. Alternatively, adifferent instrument is used for carrying the mesh and the balloon, asshown in FIG. 11B. Balloon 100 is not visible in FIGS. 11A and 11B asthe mesh is wound around the balloon.

Optionally, a second trocar 1110 is used as shown in FIG. 11B. Secondtrocar 1110 is preferably used for insertion of optics, such as anendoscope in order to provide a view of the interior of the abdominalcavity to the surgeon. Optionally, trocar 1110 is used for laparoscopicsurgical tools such as a grasper.

In general, it is preferred to make openings with as small a diameter aspossible, to prevent creation of additional hernial defects. A trocar,as compared to suture passers or a tube catcher, has a relatively largediameter, usually between 3-18 mm. Therefore, trocars 1100 and 1110 arepreferably inserted through laparoscopic openings at the side of theabdomen in order not to harm the wall at the already weakened defect.

At 1030, the mesh and balloon are released inside the abdominal cavity,as shown in FIG. 11C. Optionally, when the mesh does not slide from thewinding device, the two parts 542, 544 of knob 540 may be released asshown in FIG. 11D. This creates an opening between rods 520 and 530 andassists in sliding the mesh and balloon from the rods into the abdominalcavity.

The inflation tube is grasped inside the abdominal cavity at 1040.Preferably, a gripping device 1130, such as a suture passer, is insertedthrough a small hole in the abdominal wall to catch the inflation tube,as shown in FIG. 11E. An exemplary suture passer is EndoClose™manufactured by Covidien—Auto Suture™. In an exemplary embodiment thegripping device creates an opening 1140 in the abdominal wall which issmaller than a laparoscopic opening and does not risk any danger to theabdominal defect, even when created through the abdominal defect.Optionally, opening 1140 has a diameter no more than 1, 2, 2.5 or 2.9mm. Opening 1140 can be formed through the hernial defect or in thetissue surrounding the hernial defect.

Optionally, a grasper 1120 is also inserted through trocar 1100 andassists in bringing the inflation tube to gripping device 1130.Alternatively, the optics could pass through trocar 1100 and the grasperthrough second trocar 1110. As shown in FIG. 11E, gripping device 1130then catches loop 124 of inflation tube 120 and pulls inflation tube outof the abdominal cavity through opening 1140 at 1050. Optionally,gripping device 1130 has a hook (not shown) at its end which is adaptedto pass through loop 124. Alternatively, other grasping means, forexample a suture passer, can be used for catching loop 124 or any otherpart of inflation tube 120.

At 1055, the mesh and balloon are positioned at the hernial defect. Inan exemplary embodiment, the balloon, with the mesh attached thereto, ispositioned by pulling inflation tube 120. By pulling inflation tube 120,mesh 200 and balloon 100 are positioned close to the abdominal wall,substantially centered at the hernial defect. Optionally, hole 1140 ismade through the hernial defect, thereby assisting in centering the meshat the defect.

Alternatively, for example when the area of the defect is very thin,hole 1140 is made at the tissue surrounding the defect which is usuallythicker. The mesh may then not be precisely centered at the defect,however, the mesh should still cover the hernial defect. Optionally, theballoon and mesh can also be oriented by rotating the inflation tube,thereby ensuring that the mesh will fully cover the hernial defect.Pulling on (and optionally rotating) the inflation tube from outside thebody thus allows for convenient and accurate positioning and centeringof the mesh at a desired, predetermined position.

The position of inflation tube 120 at a central region of the balloon isconvenient for centering the mesh and balloon by the inflation tube.Alternatively, the inflation tube is not positioned at a center regionof the balloon, but off-center to some extent, which may be advantageouswhen opening 1140 is made at the surrounding of the defect, therebyenabling the larger area of the mesh to cover the hernial defect.

Optionally, loop 124 is cut off the inflation tube after extracting theinflation tube from the abdominal cavity, thereby opening the tube forreceipt of inflation fluid.

In an exemplary embodiment, a fastening adaptor 1132, optionallyprovided with gripping device 1130, is placed on the inflation tube inorder to prevent the inflation tube from sliding back into the abdominalcavity. By fastening the inflation tube in place, the surgeon can alsocontrol the desired height at which the balloon and mesh should bepositioned in the abdominal cavity. Optionally, any other fasteningmeans, such as a clamp or kelly, can be used for fastening the inflationtube in place. Gripping device 1130 is then released and an injectingdevice or pump 1150 is attached to inflation tube 120 for inflatingballoon 100 at 1060. Optionally, the inflation fluid is a gas or gasmixture, such as air or CO₂. Alternatively, any other inflation fluid,such as saline or any other liquid, may be used. Inflation of balloon100 causes the balloon to deploy. Since the balloon is attached to themesh, the deploying balloon provides a driving force to the mesh whichalso deploys and spreads as shown in FIG. 11G.

Balloon 100 and mesh 200 are positioned close to the abdominal wall andas opening 1140 was performed through the abdominal defect or in thesurrounding tissue of the defect, the mesh is situated at apredetermined position for repair of the hernial defect. Optionally,inflation tube 120 is pulled to place the mesh at the required positionand orientation.

At 1070, mesh 200 is attached to the abdominal wall. In an exemplaryembodiment, as shown in FIG. 11H, a tacker 1160 is inserted throughtrocar 1100 for fixating the mesh to the abdominal wall. Tacker 1160 maybe any suitable tacker known in the art, such as ProTack™ of Covidien,SORBAFIx™ of Davol or Davol* PermaSorb™. Alternatively, the tacker maybe inserted through second trocar 1110, while optics is inserted throughtrocar 1100. Alternatively or additionally, pins, claws, sutures,adhesive material or any other fixation means known in the art can beused for attaching mesh 200 to the abdominal wall.

In an exemplary embodiment, while the overall extent of the balloon isor may be almost comparable to the extent of the mesh, the area ofballoon 100 is substantially smaller than the area of mesh 200.Optionally, the solid area of balloon 100 is less than 10%, 20%, 30% or50% of the area of mesh 200. Optionally, balloon comprises a pluralityof connected portions separated by open areas, the open areas comprisingmore than 30%, 50% or 70% of the area of the balloon in its deflatedconfiguration. This enables the balloon to support the mesh while stillhaving a substantially smaller area than the mesh. Optionally, theextent of the balloon is also smaller than the extent of the mesh.Alternatively, the extent of the balloon may be larger than the extentof the mesh.

Optionally said balloon is characterized by a branching shape, aneccentric shape, a concentric shape, an “H” shape, a rhomboid shape, asymmetric shape, an asymmetric shape, an open shape, a closed shape orany combination thereof.

Since the area of the balloon is substantially smaller than the area ofthe mesh, and much of the central portion of the mesh is accessible fromthe back of the balloon, the surgeon can relatively freely attach themesh to the abdominal cavity, through the large open areas of theballoon without deflating or harming the balloon, while the balloon isstill attached to the mesh.

This methodology allows for support of the mesh by the balloon andcontinued positive placement of the mesh by the balloon duringattachment of the mesh to the abdominal wall. The continuing positiveplacement is also provided by the fastening adaptor holding theinflation tube in place. Since the balloon may have large open areas,the mesh can be firmly secured to the abdominal wall without attachingthe balloon to the abdominal wall and without detaching the balloon fromthe mesh. Optionally, the balloon also has a smaller extent than themesh, thereby enabling the edges of the mesh to be attached to theabdominal wall while the balloon is still attached to the mesh

Optionally, after attaching the mesh to the abdominal wall the balloonis deflated and removed from the mesh at 1080. In an exemplaryembodiment, the balloon is deflated by cutting inflation tube. Inanother exemplary embodiment, the injecting device 1150 is disconnectedfrom the inflation tube 120, thus deflating the balloon. Alternatively,injecting device 1150 is used for active deflation of the balloon. Thiscan be performed either by changing the direction of a valve at theinjecting device 1150, by pulling a plunger of a syringe like injectingdevice or by changing the direction of the pump. In an exemplaryembodiment, the balloon is removed by pulling the balloon away from themesh, as shown in FIG. 11I.

Optionally, inflation tube 120 is cut from the balloon after deflation,while the inflation tube is situated outside the body through opening1140. Optionally, inflation tube 120 is stretched before cutting, sothat the inflation tube is cut as close as possible to the balloon. Thisis preferred in order to prevent any contaminated portion of the tubewhich is outside the body from re-entering the body after cutting andavoid contamination of the abdominal cavity. Alternatively, inflationtube 120 is removed along with balloon 100 through trocar 1100 orthrough the trocar's incision.

Optionally, the balloon is removed from the mesh before completefixation of the mesh to the abdominal wall. This option is lesspreferred since the balloon, when connected to the mesh, providessupport to the mesh and assists in keeping the mesh in place. Therefore,the balloon is preferably inflated and attached to the mesh during thefixation procedure. Optionally, the balloon is deflated after removalfrom the mesh.

At 1090 the balloon is removed from the abdominal cavity through trocar1100, 1110 or through the trocar's incision.

As used herein the term “about” refers to ±10%. The terms “comprises”,“comprising”, “includes”, “including”, “having” and their conjugatesmean “including but not limited to”. This term encompasses the terms“consisting of” and “consisting essentially of”.

The phrase “consisting essentially of” means that the composition ormethod may include additional ingredients and/or steps, but only if theadditional ingredients and/or steps do not materially alter the basicand novel characteristics of the claimed composition or method.

As used herein, the singular form “a”, “an” and “the” include pluralreferences unless the context clearly dictates otherwise. For example,the term “a compound” or “at least one compound” may include a pluralityof compounds, including mixtures thereof.

The word “exemplary” is used herein to mean “serving as an example,instance or illustration”. Any embodiment described as “exemplary” isnot necessarily to be construed as preferred or advantageous over otherembodiments and/or to exclude the incorporation of features from otherembodiments.

The word “optionally” is used herein to mean “is provided in someembodiments and not provided in other embodiments”. Any particularembodiment of the invention may include a plurality of“optional”features unless such-features conflict.

Throughout this application, various embodiments of this invention maybe presented in a range format. It should be understood that thedescription in range format is merely for convenience and brevity andshould not be construed as an inflexible limitation on the scope of theinvention. Accordingly, the description of a range should be consideredto have specifically disclosed all the possible subranges as well asindividual numerical values within that range. For example, descriptionof a range such as from 1 to 6 should be considered to have specificallydisclosed subranges such as from 1 to 3, from 1 to 4, from 1 to 5, from2 to 4, from 2 to 6, from 3 to 6 etc., as well as individual numberswithin that range, for example, 1, 2, 3, 4, 5, and 6. This appliesregardless of the breadth of the range.

Whenever a numerical range is indicated herein, it is meant to includeany cited numeral (fractional or integral) within the indicated range.The phrases “ranging/ranges between” a first indicate number and asecond indicate number and “ranging/ranges from” a first indicate number“to” a second indicate number are used herein interchangeably and aremeant to include the first and second indicated numbers and all thefractional and integral numerals therebetween.

It is appreciated that certain features of the invention, which are, forclarity, described in the context of separate embodiments, may also beprovided in combination in a single embodiment. Conversely, variousfeatures of the invention, which are, for brevity, described in thecontext of a single embodiment, may also be provided separately or inany suitable subcombination or as suitable in any other describedembodiment of the invention. Certain features described in the contextof various embodiments are not to be considered essential features ofthose embodiments, unless the embodiment is inoperative without thoseelements.

Although the invention has been described in conjunction with specificembodiments thereof, it is evident that many alternatives, modificationsand variations will be apparent to those skilled in the art.Accordingly, it is intended to embrace all such alternatives,modifications and variations that fall within the spirit and broad scopeof the appended claims.

All publications, patents and patent applications mentioned in thisspecification are herein incorporated in their entirety by referenceinto the specification, to the same extent as if each individualpublication, patent or patent application was specifically andindividually indicated to be incorporated herein by reference. Inaddition, citation or identification of any reference in thisapplication shall not be construed as an admission that such referenceis available as prior art to the present invention. To the extent thatsection headings are used, they should not be construed as necessarilylimiting.

1-39. (canceled)
 40. A device for delivering a soft tissue repairprosthetic, comprising: an expandable device configured to be removablyattached with the soft tissue repair prosthetic, the expandable devicehaving a first axis and a second axis, the first axis beingsubstantially perpendicular to the second axis, the expandable devicehaving a width measurable in a direction of the second axis, wherein thesecond axis defines a maximum width of the expandable device; theexpandable device including a first outer expandable segment, a secondouter expandable segment, and an intermediate expandable segmentpositioned between the first outer expandable segment and the secondouter expandable segment, wherein the intermediate expandable segmentextends substantially in the direction of the first axis; and a firstcoil attached to the expandable device along the second axis.
 41. Thedevice of claim 40, further comprising a second coil attached to theexpandable device along the second axis.
 42. The device of claim 41,wherein the first coil is attached to the first outer expandable segmentand the second coil is attached to the second outer expandable segment.43. The device of claim 40, wherein the first coil is attached to thefirst outer expandable segment.
 44. The device of claim 40, wherein theintermediate expandable segment extends non-linearly.
 45. The device ofclaim 40, wherein each of the first and second outer expandable segmentsbow away from the intermediate expandable segment and form respectiveopenings therebetween.
 46. The device of claim 40, wherein the firstcoil is configured for removably attaching the expandable device to thesoft tissue repair prosthetic.
 47. The device of claim 40, wherein thefirst outer expandable segment, the second outer expandable segment, andthe intermediate expandable segment are arranged such that, when theexpandable device is fully expanded, a plane can intersect the firstouter expandable segment, the second outer expandable segment, and theintermediate expandable segment simultaneously.
 48. The device of claim40, wherein the first coil has a flat configuration.
 49. The device ofclaim 40, wherein the expandable device has a length measurable in adirection of the first axis, and wherein a maximum length of theexpandable device is greater than the maximum width of the expandabledevice.
 50. The device of claim 40, wherein the expandable devicecomprises an inflatable balloon.
 51. A device for delivering a softtissue repair prosthetic, comprising: an expandable device configured tobe removably attached with the soft tissue repair prosthetic, theexpandable device having a first axis and a second axis, the first axisbeing substantially perpendicular to the second axis, the expandabledevice having a length measurable in a direction of the first axis and awidth measurable in a direction of the second axis, wherein a maximumlength of the expandable device is greater than a maximum width of theexpandable device, wherein the second axis defines the maximum width ofthe expandable device; the expandable device including a first outerexpandable segment, a second outer expandable segment, and anintermediate expandable segment positioned between the first outerexpandable segment and the second outer expandable segment; and a firstcoil attached to the expandable device along the second axis.
 52. Thedevice of claim 51, further comprising a second coil attached to theexpandable device along the second axis.
 53. The device of claim 52,wherein the first coil is attached to the first outer expandable segmentand the second coil is attached to the second outer expandable segment.54. The device of claim 51, wherein the intermediate expandable segmentextends non-linearly.
 55. The device of claim 51, wherein each of thefirst and second outer expandable segments bow away from theintermediate expandable segment and form respective openingstherebetween.
 56. The device of claim 51, wherein the first coil isconfigured for removably attaching the expandable device to the softtissue repair prosthetic.
 57. The device of claim 51, wherein the firstouter expandable segment, the second outer expandable segment, and theintermediate expandable segment are arranged such that, when theexpandable device is fully expanded, a plane can intersect the firstouter expandable segment, the second outer expandable segment, and theintermediate expandable segment simultaneously.
 58. The device of claim51, wherein the first coil has a flat configuration.
 59. The device ofclaim 51, wherein the expandable device comprises an inflatable balloon.